Nuclease Fusion Protein and Uses Thereof

ABSTRACT

The present invention is concerned with nuclease fusion proteins and various uses thereof. Specifically, it relates to a polynucleotide encoding a polypeptide comprising (i) a first module comprising at least a first DNA binding domain derived from a homing endonuclease, (ii) a linker, and (iii) a second module comprising at least a second DNA binding domain and a cleavage domain derived from a restriction endonuclease, wherein said polypeptide functionally interacts only with DNA comprising a DNA recognition site for the first DNA binding domain and a DNA recognition site for the second DNA binding domain, and wherein said cleavage domain cleaves DNA within a specific DNA cleavage site upon binding of the polypeptide. Further contemplated are a vector and a non-human transgenic organism comprising said polynucleotide as well as a polypeptide encoded by the polynucleotide of the invention. Finally, the present invention relates to a method for introducing a nucleic acid of interest into a genome of a non-human organism wherein the polypeptide of the invention is applied.

The present invention is concerned with nuclease fusion proteins andvarious uses thereof. Specifically, it relates to a polynucleotideencoding a polypeptide comprising (i) a first module comprising at leasta first DNA binding domain derived from a homing endonuclease, (ii) alinker, and (iii) a second module comprising at least a second DNAbinding domain and a cleavage domain derived from a restrictionendonuclease, wherein said polypeptide functionally interacts only withDNA comprising a DNA recognition site for the first DNA binding domainand a DNA recognition site for the second DNA binding domain, andwherein said cleavage domain cleaves DNA within a specific DNA cleavagesite upon binding of the polypeptide. Further contemplated by theinvention are a vector, a non-human transgenic organism comprising saidpolynucleotide as well as a polypeptide encoded by the polynucleotide ofthe invention. Finally, the present invention relates to a method forintroducing a nucleic acid of interest into a genome of a non-humanorganism wherein the polypeptide of the invention is applied.

Restriction endonucleases are important tools for molecular cloning ofDNA. These enzymes are required for the cleavage of DNA at specificrecognition and cleavage sites, thereby allowing the reproduciblegeneration of defined DNA fragments. Moreover, said defined fragmentsgenerated by the restriction endonucleases can be combined with otherDNA molecules and, in particular, with vectors in ligation reactions forthe purpose of molecular cloning. The principles of how restrictionendonucleases can be used for molecular cloning are well known for manyyears.

Many restriction endonucleases have been characterized in the past frommany different prokaryotic organisms. There is a need for restrictionendonucleases which rarely cleave genomic DNA, i.e. those whose DNArecognition and cleavage sites occur only at a limited number in thegenome. There are rarely cleaving, naturally occurring endonucleasesknown in the art. However, most of said restriction endonucleases cleavestatistically more than once in a genome. Artificial enzymes have beenmore recently generated which statistically cleave less often andsometimes even once in a genome.

Artificial fusion proteins comprising zinc-finger domains for DNAbinding and the non-specific DNA cleavage domain of the restrictionendonuclease FokI have been reported in the prior art (Wah 1998, Proc.Natl. Acad. Sci. USA 95: 10564-10569; WO2003/080809; WO2007/139898;WO2002/057294; WO2000/27878; WO1999/45132; WO2003/062455;WO2002/057293). Instead of zinc-finger domains, transcriptionactivator-like effectors (TALEs) were reported as a suitable basis fornucleases of very high specificity when fused to the non-specific DNAcleavage domain of FokI (Christian 2010, Genetics 186(2): 757-U476).

Other approaches for generating artificial, rarely-cleavingmeganucleases are based on homing endonucleases such as LAGLIDADG homingendonucleases and, in particular, of I-CreI or I-SceI (WO2009/076292;WO2007/047859; WO2008/152524; WO2008/102198; WO2008/093249;WO2007/034262; WO2003/078619; Doyon 2006, J Am Chem Soc 128: 2477-2484).Artificial fusion proteins comprising a homing endonuclease such asI-SceI and the non-specific DNA cleavage domain of FokI have also beenreported (Lippow 2009, Nucleic Acid Res 37(9): 3061-3073).

Moreover, the rare cutting endonucleases have been reported tofacilitate homologous recombination and other integration of DNAfragments into a genome in vivo (WO2003/080809; WO2000/46386;WO2009/006297; WO2006/074956; WO2006/134496; WO2007/148964;WO2009/130695). Accordingly, these enzymes can be used for thegeneration of various types of transgenic organisms.

Thus, there is a need for further rare cutting endonucleases and, inparticular, for those which cleave at a defined DNA cleavage site andwhich produce suitable cleavage products which can be recognized andused by the endogenous DNA repair system of an organism such thatintegration of a DNA of interest into the genome of the said organismwill be facilitated.

Thus, the technical problem underlying the present invention could beseen as the provision of means and methods for complying with theaforementioned needs. The technical problem is solved by the embodimentscharacterized in the claims and herein below.

Therefore, the present invention relates to a polynucleotide encoding apolypeptide comprising:

(i) a first module comprising at least a first DNA binding domainderived from a homing endonuclease;(ii) a linker; and(iii) a second module comprising at least a second DNA binding domainand a cleavage domain derived from a restriction endonuclease;wherein said polypeptide functionally interacts only with DNA comprisinga DNA recognition site for the first DNA binding domain and a DNArecognition site for the second DNA binding domain, andwherein said cleavage domain cleaves DNA within a specific DNA cleavagesite upon binding of the polypeptide.

The term “polynucleotide” as used herein refers to single- ordouble-stranded DNA molecules as well as to RNA molecules. Encompassedby the said term is genomic DNA, cDNA, hnRNA, mRNA as well as allnaturally occurring or artificially modified derivatives of suchmolecules. The polynucleotide may be, preferably, a linear or circularmolecule. Moreover, in addition to the nucleic acid sequences encodingthe aforementioned polypeptide, a polynucleotide of the presentinvention may comprise additional sequences required for propertranscription and/or translation such as 5′- or 3′-UTR sequences.

The term “first module” as used herein refers to a first structuraland/or functional part of the polypeptide encoded by the polynucleotideof the invention. Said first module, preferably, comprises oressentially consists of at least a first DNA binding domain. DNA bindingas used herein refers to the capability of a polypeptide or domainthereof to physically bind to DNA. Such a polypeptide or domain thereofis or comprises a DNA binding domain. DNA binding occurs at a definednucleotide sequence within a DNA molecule referred to herein also as DNArecognition site of the DNA binding domain. The first module may alsocomprise, in addition to the first DNA binding domain, further domains.Such further domains, preferably, can be DNA binding domains as well orother domains which mediate interaction with regulatory proteins ortransport proteins, e.g., interaction domains for nuclear transportregulating proteins. It will be understood that, preferably, the saidfirst DNA binding domain can also be comprised in the first module as acomplete DNA binding protein, such as a naturally occurring homingendonuclease, a genetically modified homing endonuclease or anartificial fusion protein of such a homing endonuclease with another DNAbinding protein, e.g., a zinc-finger DNA binding protein or a DNAbinding transcription factor. Details of preferred DNA binding domainswhich can be applied in accordance with the present invention aredescribed elsewhere herein.

Preferably, said first module exhibits reduced or no catalytic activitywith respect to DNA cleavage. Preferably, a reduced catalytic activityas referred to in accordance with the present invention can bedetermined by measuring DNA cleavage elicited by the first module of thepolypeptide encoded by the polynucleotide of the present invention and acorresponding wild type homing endonuclease comprising the first DNAbinding domain, i.e. a comparison with respect to the DNA cleavageactivity of the homing endonuclease from which the at least first DNAbinding domain in the first module has been derived. Reduced as used inthe context of the present invention means reduced to a statisticallysignificant extent and, preferably, to a reduction of at least 70%, atleast 80%, at least 90%, at least 99%, at least 99.9%, at least 99.99%,at least 99.999%, or at least 99.9999%. Whether a reduction isstatistically significant can be determined by the skilled artisanwithout further ado by standard techniques of statistics.

The term “homing endonuclease” as used herein refers to endonucleaseswhich are typically encoded by introns or inteins. Naturally occurringhoming endonucleases, similar to transposons, allow for the perpetuationof the genetic elements that encode them in that they, usually, cleavethe DNA of the intron- or intein-less allele of the recipient organism.The DNA recognition sites of homing endonucleases are long enough tooccur randomly only with a very low probability, preferablyapproximately once every 10⁷ bp up to once every 10⁹ bp or even with alower probability. Preferably, the DNA recognition sites recognized bythe DNA binding domains of homing endonucleases, in contrast to those ofother endonucleases, consist of at least 10, at least 12, at least 14,at least 16, at least 18, at least 20, at least 30 or at least 40contiguous nucleotides. Preferably, said recognition sites areasymmetric. Upon cleavage of the DNA of the intro- or intein-lessallele, the cellular DNA repair system is activated, whereby the intron-or intein containing gene is supplied in trans, the so called “homing”process.

There are five different families of homing endonucleases. The membersof the LAGLIDADG family of homing endonucleases each have one or twoLAGLIDADG motifs per polypeptide chain. The LAGLIDADG amino acidsequence is a conserved sequence directly involved in domain-domain andsubunit-subunit interaction and the DNA cleavage process. Those enzymesthat have only one motif per polypeptide chain act as homodimers, whilethose having two motifs act as monomers. The members of the GIY-YIGfamily of homing endonucleases have one GIY-YIG motif as the catalyticmotif that is associated with a DNA binding motif. The prototypic enzymeof this family is I-TevI. The members of the His-Cys box family ofhoming endonucleases contain a stretch of 30 amino acids including twoconserved histidines and three conserved cysteins. I-PpoI is a member ofsaid family and acts as a monomer. The members of the H-N-H family ofhoming endonucleases are characterized by a consensus sequence ofapproximately 30 amino acids having two pairs of conserved histidinesand one asparagine. The said conserved amino acids form analpha-beta-beta-alpha (αββα) metal finger motif. The PD . . . D/EXKfamily of homing endonucleases are characterized by a structural corethat consists of a four-stranded beta sheet flanked by alpha helicesthat harbors the characteristic PD . . . D/EXK active site motif (see,e.g., Pingoud 2005, Cell Mol Life Sci 62(6): 685-707).

As referred to above, a first DNA binding domain according to theinvention is a DNA binding domain of a homing endonuclease. Preferredhoming endonucleases from which such a first DNA binding domain can bederived are selected from the group consisting of: LAGLIDADG-familyhoming endonucleases, GIY-YIG family homing nucleases, His-Cys-boxfamily homing endonucleases, H-N-H family homing endonucleases and PD .. . D/EXK family homing endonucleases. Preferred members of said homingendonuclease families which can be used for deriving DNA binding domainsto be included into the polypeptide encoded by the polynucleotide of thepresent invention are F-CphI, F-EcoT5I, F-EcoT5II, F-EcoT5IV, F-PhiU5I,F-SceI, F-SceII, F-TevI, F-TevII, F-TevIII, F-TevIV, H-DreI, I-AniI,I-ApeKI, I-BanI, I-BasI, I-BmoI, I-BthII, I-BthORFAP, I-CeuI, I-ChuI,I-CmoeI, I-CpaI, I-CpaII, I-CreI, I-CreII, I-CsmI, I-CvuI, I-DdiI,I-DmoI, I-HmuI, I-HmuII, I-LIaI, I-LtrI, I-LtrWI, I-MsoI, I-NanI,I-NitI, I-NjaI, I-OnuI, I-PakI, I-PogI, I-PorI, I-PpoI, I-ScaI, I-SceI,I-SceII, I-SceIII, I-SceIV, I-SceV, I-SceVI, I-SceVII, I-SpomI,I-Ssp6803I, I-TevI, I-TevII, I-TevIII, I-Tsp061I, I-TwoI, I-Vdi141I,PI-MgaI, PI-MIeSI, PI-MtuI, PI-PabI, PI-PabII, PI-PfuI, PI-PfuII,PI-PkoI, PI-PkoII, PI-PspI, PI-ScaI, PI-SceI, PI-TfuI, PI-TfuII,PI-ThyI, PI-TliI, PI-TliII, PI-TmaI, PI-TmaKI, and PI-ZbaI.

More preferably, said first DNA binding domain comprised in the firstmodule is derived from a homing endonuclease of the LAGLIDADG-family.Even more preferably, said first DNA binding domain comprised in thefirst module is derived from I-SceI. Most preferably, said DNA bindingdomain is derived from I-SceI or a variant thereof and comprises atleast one of following modifications: substitution D44S alone or incombination with D145A, or substitution D44N in combination with D145A.The positions of the modifications referred to before are indicated forthe wild type I-SceI protein. These modifications inactivate thecatalytic domain of I-SceI which is required for DNA cleavage so thatthe modified I-SceI either lacks the capability to cleave DNA or atleast has reduced DNA cleavage activity while the DNA binding propertiesare essentially maintained. It is to be understood that theaforementioned amino acid positions will vary if modified variants ofthe I-SceI protein are used. Nevertheless, it is envisaged that DNAbinding domains from such variants, preferably, also comprise at leastone of the modifications at a corresponding position in their amino acidsequences which, preferably, also results in a loss or reduction of theDNA cleavage activity. The DNA cleavage activity of a modified variantcan be determined by the skilled artisan without further ado, e.g., byusing the assays described in the accompanying Examples, below. Theamino acid sequence of I-SceI is well known in the art and described,e.g., in Pingoud 2005, loc cit. Moreover, nucleic acid sequencesencoding said I-SceI amino acid sequences have also been described andcan be derived from the amino acid sequence by the skilled artisanwithout further ado taking into account the degeneracy of the geneticcode.

In a particular preferred embodiment, said I-SceI wild type sequence hasan amino acid sequence as shown in SEQ ID NO: 1 or is a variant thereofhaving an amino acid sequence which differs from SEQ ID NO: 1 by atleast one amino acid substitution, deletion and/or addition.

Preferably, such a variant of I-SceI has an amino acid sequence which isat least 70%, at least 80%, at least 90%, at least 95%, at least 98% orat least 99% identical with SEQ ID NO: 1 and, preferably, comprises aDNA binding domain having essentially the same DNA binding activity asthe DNA binding domain of I-SceI shown in SEQ ID NO: 1. Sequenceidentity as used herein is, preferably, to be determined by way ofalignment over the entire length of an amino acid or nucleic acidsequence or over a contiguous stretch of amino acids or nucleotides,respectively. Said stretch being at least 50% in length of the referencesequence to which a given sequences shall be compared. A preferredalgorithm for determining the percentage of sequence identity is theNeedleman and Wunsch algorithm (Needleman 1970, J. Mol. Biol.(48):444-453) which has been incorporated into the needle program in theEMBOSS software package (EMBOSS: The European Molecular Biology OpenSoftware Suite, Rice 2000, Trends in Genetics 16(6), 276-277), usingeither a BLOSUM 45 or PAM250 scoring matrix for distantly relatedproteins, or either a BLOSUM 62 or PAM160 scoring matrix for moreclosely related proteins, and a gap opening penalty of 16, 14, 12, 10,8, 6, or 4 and a gap extension penalty of 0.5, 1, 2, 3, 4, 5, or 6.Guides for local installation of the EMBOSS package as well as links toWEB-Services can be found at http://emboss.sourceforge.net. Preferredparameters to be used for aligning two amino acid sequences using theneedle program are the default parameters, including the EBLOSUM62scoring matrix, a gap opening penalty of 10 and a gap extension penaltyof 0.5. Also preferably, the percent identity between two nucleotidesequences is determined using the needle program in the EMBOSS softwarepackage, using the EDNAFULL scoring matrix and a gap opening penalty of16, 14, 12, 10, 8, 6, or 4 and a gap extension penalty of 0.5, 1, 2, 3,4, 5, or 6. Further preferred parameters to be used in conjunction foraligning two nucleic acid sequences using the needle program are thedefault parameters, including the EDNAFULL scoring matrix, a gap openingpenalty of 10 and a gap extension penalty of 0.5. The nucleic acid andprotein sequences of the present invention can further be used as a“query sequence” to perform a search against public databases to, forexample, identify other family members or related sequences. Suchsearches can be performed using the BLAST series of programs (version2.2) of Altschul et al. (Altschul 1990, J. Mol. Biol. 215:403-10).

Preferably, a variant of I-SceI as referred to herein includes thosevariants which are encoded by a nucleic acid which hybridizesspecifically and, preferably, under stringent conditions, with a nucleicacid encoding the amino acid sequence shown in SEQ ID NO: 1. Thesestringent conditions are known to the skilled artisan and can be foundin Current Protocols in Molecular Biology, John Wiley & Sons, N.Y.(1989), 6.3.1-6.3.6. Preferred stringent hybridization conditions arehybridization conditions in 6× sodium chloride/sodium citrate (=SSC) atapproximately 45° C., followed by one or more washing steps in 0.2×SSC,0.1% SDS at 50 to 65° C. The skilled artisan knows that thesehybridization conditions differ depending on the type of nucleic acidand, for example when organic solvents are present, with regard to thetemperature and concentration of the buffer. For example, under“standard hybridization conditions” the temperature differs depending onthe type of nucleic acid between 42° C. and 58° C. in aqueous bufferwith a concentration of 0.1 to 5×SSC (pH 7.2). If organic solvent ispresent in the abovementioned buffer, for example 50% formamide, thetemperature under standard conditions is approximately 42° C. Thehybridization conditions for DNA:DNA hybrids are, preferably, 0.1×SSCand 20° C. to 45° C., preferably between 30° C. and 45° C. Thehybridization conditions for DNA:RNA hybrids are, preferably, 0.1×SSCand 30° C. to 55° C., preferably between 45° C. and 55° C. Theabovementioned hybridization temperatures are determined for example fora nucleic acid with approximately 100 bp (=base pairs) in length and aG+C content of 50% in the absence of formamide. The skilled artisanknows how to determine the hybridization conditions required byreferring to textbooks such as the textbook mentioned above, or thefollowing textbooks: Sambrook et al., “Molecular Cloning”, Cold SpringHarbor Laboratory, 1989; Hames and Higgins (Ed.) 1985, “Nucleic AcidsHybridization: A Practical Approach”, IRL Press at Oxford UniversityPress, Oxford; Brown (Ed.) 1991, “Essential Molecular Biology: APractical Approach”, IRL Press at Oxford University Press, Oxford.Alternatively, polynucleotide variants are obtainable by PCR-basedtechniques such as mixed oligonucleotide primer-based amplification ofDNA, i.e. using degenerated primers against conserved domains of thepolypeptides of the present invention. Conserved domains of thepolypeptide of the present invention may be identified by a sequencecomparison of the nucleic acid sequences of the polynucleotides or theamino acid sequences of the polypeptides of the present invention.Oligonucleotides suitable as PCR primers as well as suitable PCRconditions are described in the accompanying Examples. As a template,DNA from yeast, preferably, from Saccharomyces cervisiae, may be used.

Preferably, envisaged by the present invention are also shortened I-SceIpolypeptides which differ from SEQ ID NO: 1 or its aforementionedvariants in that between 5 and 9 C-terminal amino acids, preferably atleast the 5, 6, 7, 8 or up to all 9 C-terminal amino acids, are deleted.

The term “second module” as used herein refers to a second structuraland/or functional part of the polypeptide encoded by the polynucleotideof the invention. Said second module, preferably, comprises oressentially consists of at least a second DNA binding domain and acleavage domain derived from a restriction endonuclease. A cleavagedomain as referred to herein is capable of cleaving a DNA molecule at aspecific DNA cleavage site. A specific DNA cleavage site as referred toin accordance with the present invention refers to a site which isrecognized by the cleavage domain and cleaved between predefinednucleotides. In contrast, some endonucleases have a cleavage domainwhich cleaves the DNA at a certain position regardless of thenucleotides present at this position. A prototype endonuclease whichexhibits such unspecific cleavage is FokI. The second module may alsocomprise, in addition to the second DNA binding domain and cleavagedomain, further domains. Such further domains, preferably, can be DNAbinding domains as well domain mediating interaction between two secondmodules, or other domains which mediate interaction with regulatoryproteins or transport proteins, e.g., interaction domains for nucleartransport regulating proteins. It will be understood that, preferably,the said second DNA binding domain and/or the cleavage domain can alsobe comprised in the second module as a complete endonuclease protein,such as a naturally occurring restriction endonuclease or a geneticallymodified endonuclease. Moreover, it is well known that restrictionendonucleases and, in particular, the type II restriction endonucleasessaid, bind to DNA—with very few exceptions—as a homodimer. Accordingly,a DNA binding domain and cleavage domains as referred to herein may befound as a consequence of the homodimerization of two restrictionendonuclease subunits. Preferably, the specific DNA cleavage site andsaid DNA recognition site of the second DNA binding domain of therestriction endonuclease are identical. Also preferably, said second DNAbinding domain and the cleavage domain comprised in the second moduleare derived from a restriction endonuclease which exhibits reduced DNAbinding and/or reduced catalytic activity when compared to the wild typerestriction endonuclease. Details of preferred DNA binding domains to beapplied in accordance with the present invention are described elsewhereherein. Also preferably, envisaged in accordance with the presentinvention are second modules which have a reduced capability of forminghomodimers in the absence of the DNA recognition site. In particular, itis envisaged that in a particular preferred embodiment, a functionalhomodimer of the polypeptide as referred to herein above is only formedwhen the two polypeptide monomers are recruited to the corresponding DNArecognition sites. Thereby, unspecific DNA binding can be preventedwhich may occur due to the formation of a homodimer as a consequence ofbinding of one monomer to its corresponding recognition site andsubsequent dimerization of a second monomer resulting fromprotein-protein interactions between the monomers rather than specificDNA binding.

Preferred endonucleases from which the second DNA binding domain and theDNA cleavage domain comprised in the second module can be derived aretype IIP restriction endonucleases (see Pingoud 2005, loc cit). Therecognition sites in a DNA molecule recognized by the DNA bindingdomains of such endonucleases, in contrast to those of theaforementioned homing endonucleases, consist of at least four, at leastsix or up to eight contiguous nucleotides. Preferably, said recognitionsites are palindromic. Moreover, preferably, the type IIP enzymes cleavethe DNA within the DNA recognition site or immediately adjacent thereto.The said DNA recognition site is found rather frequently in a genome.Preferred type IIP restriction endonucleases as referred to herein areselected from the group consisting of: PvuII, EcoRV BamHI, BcnI,BfaSORF1835P, BfiI, BgII, BgIII, BpuJI, Bse634I, BsoBI, BspD6I, BstYI,Cfr10I, EcI18kI, EcoO109I, EcoRI, EcoRII, EcoRV, EcoR124I, EcoR124II,HinP1I, HincII, HindIII, Hpy99I, Hpy188I, MspI, MunI, MvaI, NaeI,NgoMIV, NotI, OkrAI, PabI, PacI, PspGI, PvuII, Sau3AI, SdaI, SfiI,SgrAI, ThaI, VvuYORF266P, DdeI, Eco57I, HaeIII, HhaII, HindII, and NdeI.More preferably, said type IIP restriction endonucleases or the DNAbinding and cleavage domains derived therefrom are modified as to showno or at least reduced star activity, a reduced DNA binding with respectto their DNA recognition site (K_(m)) and/or a reduced DNA cleavageactivity (k_(cat)) of the cleavage domain. More preferably, it isenvisaged that in one embodiment the type II restriction endonuclease orthe domains derived therefrom have a reduced capability of forminghomodimers in the absence of the DNA recognition site. Suitablerestriction endonucleases or domains thereof for this purposes can beobtained, e.g., by random mutagenesis and subsequent testing fordimerization in the presence and absence of the DNA recognition site.Those variants which dimerize only in the presence but not in theabsence of the DNA recognition site can be identified and used for thepolypeptide encoded by the polynucleotide of the present invention.

Most preferably, the endonuclease envisaged in accordance with thepresent invention is PvuII or a genetically modified variant thereofand, thus, said second DNA binding domain and the cleavage domaincomprised in the second module are derived from PvuII. More preferably,the said second DNA binding domain and the cleavage domain comprised inthe second module are derived from PvuII or a variant thereof andcomprise at least one of following modifications: substitution T46G,substitution H83A, substitution Y94F, substitution T46G in combinationwith H83A, substitution T46G in combination with Y94F or substitutionT46G in combination with H83A and Y94F. The positions of themodifications referred to before are indicated for the wild type PvuIIprotein. However, it is to be understood that these positions will varyif modified variants of the PvuII protein are used. Nevertheless, it isenvisaged that DNA binding domains from such variants, preferably, alsocomprise at least one of the modifications at a corresponding positionin their amino acid sequences. The amino acid sequence of PvuII is wellknown in the art and described, e.g., in Athanasiadis 1990, Nucleic acidRes 18(21): 6434. Moreover, nucleic acid sequences encoding said PvuIIamino acid sequences have also been described and can be derived fromthe amino acid sequence by the skilled artisan without further adotaking into account the degeneracy of the genetic code.

In a particular preferred embodiment, the PvuII wild type sequencereferred to in accordance with the present invention has an amino acidsequence as shown in SEQ ID NO: 2 or is a variant thereof having anamino acid sequence which differs from SEQ ID NO: 2 by at least oneamino acid substitution, deletion and/or addition.

Preferably, such a variant of PvuII has an amino acid sequence which isat least 70%, at least 80%, at least 90%, at least 95%, at least 98% orat least 99% identical with SEQ ID NO: 2 and, preferably, comprises aDNA binding domain having essentially the same DNA binding and cleavageproperties as the DNA binding and cleavage domain of PvuII having SEQ IDNO: 2. How to determine said sequence identity is described elsewhereherein in detail.

Preferably, variants of PvuII as referred to herein include thosevariants which are encoded by a nucleic acid which hybridizesspecifically and, preferably, under stringent conditions, with a nucleicacid encoding the amino acid sequence shown in SEQ ID NO: 2. Preferredstringent hybridization conditions are described elsewhere herein indetail. Alternatively, polynucleotide variants are obtainable byPCR-based techniques such as mixed oligonucleotide primer-basedamplification of DNA, i.e. using degenerate primers against conserveddomains of the polypeptides of the present invention. Conserved domainsof the polypeptide of the present invention may be identified by asequence comparison of the nucleic acid sequences of the polynucleotidesor the amino acid sequences of the polypeptides of the presentinvention. Oligonucleotides suitable as PCR primers as well as suitablePCR conditions are described in the accompanying Examples. As atemplate, DNA from bacteria and, preferably, Proteus vulgaris, may beused.

Within the polypeptide encoded by the polynucleotide of the presentinvention, the first module is separated from the second module by alinker. Said linker, preferably, is a flexible structure of sufficientlength allowing the DNA binding domains comprised in the modules tointeract with their DNA binding sites and allowing the DNA cleavagedomain to cleave the DNA. Flexible linker structures to be used in thepolypeptide encoded by the polynucleotide of the present invention,preferably, consist of five to twenty, more preferably, six to ten aminoacids or more, i.e. at least six, at least seven, at least eight, atleast nine or ten or more amino acids. Preferably, said linker has anamino acid sequence as shown in SEQ ID NO: 3 (ASRTTG) or SEQ ID NO: 4(ASTKQLVKSG). Alternatively, the linker may have an amino acid sequenceas in SEQ ID NO: 5 (ASGGSGSGSG) or SEQ ID NO: 6 (ASGDSGSDSG).

The polypeptide encoded by the polynucleotide of the invention shallfunctionally interact only with DNA comprising a DNA recognition sitefor the first DNA binding domain and the DNA recognition site for thesecond DNA binding domain. Accordingly, neither the first DNA bindingdomain nor the second DNA binding domain shall be, preferably,sufficient for allowing a functional interaction of the polypeptideencoded by the polynucleotide of the invention with DNA. A functionalinteraction as used herein refers to specific DNA binding to the DNAbinding sites such that the cleavage domain can cleave at its specificDNA cleavage site upon binding. In order to be functional, thepolypeptide according to the invention will form a homodimer comprisingtwo polypeptide monomers as having the structure of the polypeptide ofthe invention. The second modules of the two polypeptides physicallyinteract with each other. The second modules are then capable of bindingto the second DNA recognition site in dimerized form. Thus, thepolypeptide of the invention in its dimerized functional form recognizesa tripartite DNA recognition site which comprises the recognition siteof the second DNA binding domain flanked by a recognition site for thefirst DNA binding domain at its 5′ and its 3′ ends. Upon specificbinding to said tripartite DNA recognition site, the polypeptide via itsDNA cleavage domain shall cleave the DNA within the said specificcleavage site or adjacent thereto. Preferably, said cleavage site andthe second DNA binding site are identical. Thus, the DNA is cleaved atdefined nucleotides within the cleavage site or adjacent thereto by thepolypeptide according to the present invention.

A preferred polynucleotide of the present invention encodes apolypeptide that comprises (i) a first module comprising at least theDNA binding domain derived from I-SceI and, preferably, an inactivevariant of I-SceI as specified above, (ii) a linker having SEQ ID NO: 3or 4; and (iii) a second module comprising at least a second DNA bindingdomain and a cleavage domain derived from PvuII and, preferably, a PvuIIvariant as specified above wherein the DNA binding and cleavage domainare modified as to show no or at least reduced star activity, to have areduced DNA binding with respect to their DNA recognition site and/or toexhibit reduced DNA cleavage by the cleavage domain. The polypeptideencoded by such a polynucleotide shall functionally interact only withDNA comprising a DNA recognition site for the first DNA binding domainof I-SceI and the DNA recognition site for the second DNA binding domainderived from PvuII. Since PvuII will form a homodimer in order to forman active enzyme, it will be understood that the DNA binding siterecognized by the polypeptide is a tripartite DNA binding sitecomprising a PvuII DNA binding site flanked at the 5′ and the 3′ end bya I-SceI DNA binding site (I-SceI DNA recognition site-PvuII DNArecognition site-I-SceI DNA recognition site). Moreover, the polypeptidewill cleave DNA within a specific DNA cleavage site upon binding, i.e.within defined positions and nucleotides of the PvuII binding site.

More preferably, the polynucleotide of the present invention encodingsuch a polypeptide comprises a nucleic acid sequence as shown in any oneof SEQ ID NOs: 7 or 8 or which encodes a polypeptide comprising an aminoacid sequence as shown in any one of SEQ ID NOs: 9 or 10. Variantpolynucleotides having a nucleic acid sequence which differs from SEQ IDNOs: 7 or 8 or encoding an amino acid sequence which differs from SEQ IDNOs: 9 or 10 by at least one nucleotide or amino acid substitution,deletion and/or addition are also encompassed by the present invention.Preferably, such a variant has a nucleic acid sequence which is at least70%, at least 80%, at least 90%, at least 95%, at least 98% or at least99% identical with SEQ ID NOs: 7 or 8 or an amino acid sequence which isat least 70%, at least 80%, at least 90%, at least 95%, at least 98% orat least 99% identical with SEQ ID NOs: 9 or 10. Such variants,preferably, comprise the aforementioned first and second modules as wellas the linker. How to determine said sequence identity is describedelsewhere herein in detail. Also preferably, variants as referred toherein include those variants which are encoded by a nucleic acid whichhybridizes specifically and, preferably, under stringent conditions,with a nucleic acid encoding the amino acid sequence shown in SEQ ID NO:7 or 8 or to a nucleic acid encoding an amino acid sequence as shown inSEQ ID NOs: 9 or 10. Again, such variants, preferably, comprise thestructural characteristics of the aforementioned first and secondmodules as well as the linker.

Advantageously, the present invention provides a polynucleotide whichencodes a polypeptide capable of specifically recognizing anartificially composed tripartite DNA recognition sequence and which iscapable of cleaving a DNA comprising such tripartite DNA recognitionsequence within a specific DNA cleavage site, i.e. at a defined positionbetween predefined nucleotides. Since the tripartite DNA recognitionsequence is a rather large sequence, it will presumably occur onlyrarely within a natural occurring genome. Preferably, the saidtripartite DNA recognition site occurs statistically less than once pergenome. As a consequence, the polypeptide according to the presentinvention shall cleave the genome only rarely and, preferably, once,i.e. at the tripartite DNA recognition site. Thereby, the polypeptidecan facilitate integration of heterologous DNA, e.g., a transgene, at acertain locus within the genomic DNA that can be easily identified afterthe integration took place. Moreover, homologous recombination eventscan be facilitated as well. Thanks to the present invention, thegeneration of transgenic organisms, such as transgenic microorganisms,transgenic plants or transgenic animals, will be significantly improved.The polypeptide of the present invention, however, can also be used as atool for mere DNA cleavage, i.e. as a rare cutting endonuclease specificfor the aforementioned artificial tripartite DNA recognition site. Sucha rare cutting endonuclease can, of course, be applied for allconventional cloning approaches. The polynucleotide of the presentinvention encodes a polypeptide which has an improved specificitycompared to zinc finger nucleases or TALe nucleases as well as so-calledartificial meganucleases since it recognizes an extended tripartite DNArecognition site as described above. Moreover, it has been found thateven blunt end cutters, such as PvuII, can be used for generating thepolypeptide of the present invention. This is somewhat surprising sinceit was reported previously that blunt ends introduced into genomic DNAby blunt end cutting endonucleases such as PvuII may be poor substratesfor the repair system in some organisms (Westmoreland 2010, DNA Repair9: 617-626).

The explanations and definitions given for the terms above apply mutatismutandis for the following embodiments of the invention.

The present invention also relates to a vector comprising thepolynucleotide of the present invention.

The term “vector” as used herein encompasses phage, plasmid, viral orretroviral vectors as well as artificial chromosomes, such as bacterialor yeast artificial chromosomes. The vector encompassing thepolynucleotides of the present invention, preferably, further comprisesselectable markers for propagation and/or selection in a host. Vectorscan be introduced into prokaryotic and eukaryotic cells via conventionaltransformation or transfection techniques. The terms “transformation”and “transfection”, conjugation and transduction, as used in the presentcontext, are intended to comprise a multiplicity of methods known in theprior art for the introduction of foreign nucleic acid (for example DNA)into a host cell, including calcium phosphate or calcium chloridecoprecipitation, DEAE-dextran-mediated transfection, lipofection,natural competence, chemically mediated transfer, electroporation orparticle bombardment. Suitable methods for the transformation ortransfection of host cells, including plant cells, can be found inSambrook et al. (Molecular Cloning: A Laboratory Manual, 2nd ed., ColdSpring Harbor Laboratory, Cold Spring Harbor Laboratory Press, ColdSpring Harbor, N.Y., 1989) and other laboratory textbooks such asMethods in Molecular Biology, 1995, Vol. 44, Agrobacterium protocols,Ed.: Gartland and Davey, Humana Press, Totowa, N.J. Alternatively, aplasmid vector may be introduced by heat shock or electroporationtechniques. Should the vector be a virus, it may be packaged in vitrousing an appropriate packaging cell line prior to application to hostcells. Retroviral vectors may be replication competent or replicationdefective. In the latter case, viral propagation generally will occuronly in complementing host cells.

Suitable cloning vectors are generally known to the skilled worker. Inparticular, they include vectors which can replicate in microbialsystems. These vectors, preferably, ensure efficient cloning inbacteria, yeasts or fungi.

Preferably, in the vector of the invention the polynucleotide isoperatively linked to an expression control sequences allowingexpression in prokaryotic or eukaryotic host cells or isolated fractionsthereof. Thus, preferably, the vector of the present invention is anexpression vector. Expression of the polynucleotide comprisestranscription of the polynucleotide into a translatable mRNA. Regulatoryelements ensuring expression in host cells are well known in the art.Preferably, they comprise regulatory sequences ensuring initiation oftranscription and/or poly-A signals ensuring termination oftranscription and stabilization of the transcript. Additional regulatoryelements may include transcriptional as well as translational enhancers.Possible regulatory elements permitting expression in prokaryotic hostcells comprise, e.g., the lac-, trp- or tac-promoter in E. coli, andexamples for regulatory elements permitting expression in eukaryotichost cells are the AOX1- or the GAL1-promoter in yeast or the CMV-,SV40-, RSV-promoter (Rous sarcoma virus), CMV-enhancer, SV40-enhancer ora globin intron in mammalian and other animal cells. Moreover, inducibleexpression control sequences may be used in an expression vectorencompassed by the present invention. Such inducible vectors maycomprise tet or lac operator sequences or sequences inducible by heatshock or other environmental factors. Suitable expression controlsequences are well known in the art. Beside elements which areresponsible for the initiation of transcription such regulatory elementsmay also comprise transcription termination signals, such as theSV40-poly-A site or the tk-poly-A site, downstream of thepolynucleotide.

Preferably, the expression of proteins in prokaryotes, preferably,involves the use of vectors comprising constitutive or induciblepromoters which govern the expression of fusion or nonfusion proteins.Typical fusion expression vectors are, inter alia, pGEX (GE Healthcare,Piscataway, N.J.; Smith 1988, Gene 67:31-40), pMAL (New England Biolabs,Ipswich, Mass.) and pRIT5 (GE Healthcare, Piscataway, N.J.), whereglutathione S-transferase (GST), maltose-E-binding protein and proteinA, respectively, is fused with the recombinant target protein. Examplesof suitable inducible nonfusion E. coli expression vectors are, interalia, pTrc (Amann 1988, Gene 69:301-315) and pET 11d (Studier et al.,Gene Expression Technology: Methods in Enzymology 185, Academic Press,San Diego, Calif. (1990) 60-89). The target gene expression from thepTrc vector is based on the transcription from a hybrid trp-lac fusionpromoter by the host RNA polymerase. The target gene expression from thevector pET 11d is based on the transcription of a T7-gn10-lac fusionpromoter, which is mediated by a viral RNA polymerase (T7 gn1), which iscoexpressed. This viral polymerase is provided by the host strains BL21(DE3) or HMS174 (DE3) from a resident λ-prophage which harbors a T7 gn1gene under the transcriptional control of the lacUV 5 promoter. Othervectors which are suitable for prokaryotic organisms are known to theskilled worker, these vectors are, for example in E. coli pLG338,pACYC184, the pBR series such as pBR322, the pUC series such as pUC18 orpUC19, the M113mp series, pKC30, pRep4, pHS1, pHS2, pPLc236, pMBL24,pLG200, pUR290, pIN-III113-B1, λgt11 or pBdCI, in Streptomyces pIJ101,pIJ364, pIJ702 or pIJ361, in Bacillus pUB110, pC194 or pBD214, inCorynebacterium pSA77 or pAJ667.

Also preferably encompassed herein are yeast expression vectors.Examples for vectors for expression in the yeast S. cerevisiae comprisepYeDesaturasec1 (Baldari 1987, EMBO J. 6:229-234), pMFa (Kurjan 1982,Cell 30:933-943), pJRY88 (Schultz 1987, Gene 54:113-123) and pYES2(Invitrogen Corporation, San Diego, Calif.). Vectors and processes forthe construction of vectors which are suitable for use in other fungi,such as the filamentous fungi, comprise those which are described indetail in: van den Hondel, C. A. M. J. J., & Punt, P. J. (1991) “Genetransfer systems and vector development for filamentous fungi, in:Applied Molecular Genetics of fungi, J. F. Peberdy et al., Ed., pp.1-28, Cambridge University Press: Cambridge, or in: More GeneManipulations in Fungi [J. W. Bennet & L. L. Lasure, Ed., pp. 396-428:Academic Press: San Diego]. Further suitable yeast vectors are, forexample, pAG-1, YEp6, YEp13 or pEMBLYe23.

As an alternative, the polynucleotides according to the invention canalso be expressed in insect cells using Baculovirus expression vectors.Baculovirus vectors which are available for the expression of proteinsin cultured insect cells (for example Sf9 cells) comprise the pAc series(Smith 1983, Mol. Cell. Biol. 3:2156-2165) and the pVL series (Lucklow1989, Virology 170:31-39).

Suitable expression vectors for eukaryotic cells which are alsopreferably encompassed by the present invention are known in the artsuch as Okayama-Berg cDNA expression vector pcDV1 (Pharmacia),pBluescript (Stratagene), pCDM8, pRc/CMV, pcDNA1, pcDNA3 (Invitrogen) orpSPORT1 (Invitrogen). Expression vectors can also be derived fromviruses such as retroviruses, vaccinia virus, adeno-associated virus,herpes viruses, or bovine papilloma virus, may be used for delivery ofthe polynucleotide or vector of the invention into a targeted cellpopulation. Methods which are well known to those skilled in the art canbe used to construct recombinant viral vectors; see, for example, thetechniques described in Sambrook, Molecular Cloning A Laboratory Manual,Cold Spring Harbor Laboratory (1989) N.Y. and Ausubel, Current Protocolsin Molecular Biology, Green Publishing Associates and WileyInterscience, N.Y. (1994).

Preferred plant expression vectors comprise those which are described indetail in: Becker 1992, Plant Mol. Biol. 20:1195-1197; and Bevan 1984,Nucl. Acids Res. 12:8711-8721; Vectors for Gene Transfer in HigherPlants; in: Transgenic Plants, Vol. 1, Engineering and Utilization, Ed.:Kung and R. Wu, Academic Press, 1993, p. 15-38. A plant expressioncassette preferably comprises expression control sequences which arecapable of governing the expression of genes in plant cells and whichare linked operably so that each sequence can fulfill its function, suchas transcriptional termination, for example polyadenylation signals.Preferred polyadenylation signals are those which are derived fromAgrobacterium tumefaciens T-DNA, such as gene 3 of the Ti plasmidpTiACH5 (Gielen 1984, EMBO J. 3: 835 ff), which is known as octopinesynthase, or functional equivalents thereof, but all other terminatorswhich are functionally active in plants are also suitable. Since plantgene expression is very often not limited to the transcriptional level,a plant expression cassette preferably comprises other sequences whichare linked operatively, such as translation enhancers, for example theoverdrive sequence, which comprises the tobacco mosaic virus5′-untranslated leader sequence, which increases the protein/RNA ratio(Gallie 1987, Nucl. Acids Research 15:8693-8711). As described above,plant gene expression must be linked operably with a suitable promoterwhich triggers gene expression with the correct timing or in a cell- ortissue-specific manner. Utilizable promoters are constitutive promoters(Benfey 1989, EMBO J. 8: 2195-2202), such as those which are derivedfrom plant viruses, such as 35S CAMV (Franck 1980, Cell 21: 285-294),19S CaMV (see also U.S. Pat. No. 5,352,605 and WO 84/02913), or plantpromoters, such as the promoter of the small Rubisco subunit, which isdescribed in U.S. Pat. No. 4,962,028. Other preferred sequences for usein operable linkage in plant gene expression cassettes are targetingsequences, which are required for steering the gene product into itscorresponding cell compartment (see a review in Kermode 1996, Crit. Rev.Plant Sci. 15, 4: 285-423 and references cited therein), for exampleinto the vacuole, into the nucleus, all types of plastids, such asamyloplasts, chloroplasts, chromoplasts, the extracellular space, themitochondria, the endoplasmic reticulum, oil bodies, peroxisomes andother compartments of plant cells.

Gene expression can also be facilitated via a chemically induciblepromoter (see review in Gatz 1997, Annu. Rev. Plant Physiol. Plant Mol.Biol., 48:89-108). Chemically inducible promoters are particularlysuitable when it is desired that gene expression should take place in atime-specific manner. Examples of such promoters are a salicylicacid-inducible promoter (WO95/19443), a tetracycline-inducible promoter(Gatz 1992, Plant J. 2, 397-404) and an ethanol-inducible promoter.

The present invention contemplates a non-human organism comprising thepolynucleotide or the vector of the present invention.

The term “non-human organism” as used herein relates to any organismexcept human beings. Accordingly, the non-human organism, preferably, isa microorganism, a plant, plant part or isolated cell thereof, or ananimal, animal tissue or isolated cell thereof. Moreover, eukaryotic orbacterial host cells are encompassed as non-human organisms as well. Thenon-human organism may comprise the polynucleotide of the invention orthe vector of the invention for the purpose of DNA propagation as wellas for the purpose of expressing the polypeptide according to thisinvention or both. The polynucleotide or vector may be presentintegrated into the genome of the host or present in an episomal form.Further preferred non-human organisms according to the present inventionare described in the following.

Preferred microorganisms are prokaryotic and eukaryotic microorganismsand, in particular, are selected from bacteria, fungi, yeast or cellculture cells from any one of the non-human animals or plants specifiedbelow.

Preferred non-human animals include mammals, birds, reptiles, fish,nematodes, and insects. More preferably, the non-human animal is amammal and, in particular, a rat, a mouse, a rabbit, a dog, a cat or afarming animal, such as a pig, a horse, a sheep or a cow.

Preferred plants are selected from the group of the plant familiesAdelotheciaceae, Anacardiaceae, Asteraceae, Apiaceae, Betulaceae,Boraginaceae, Brassicaceae, Bromeliaceae, Caricaceae, Cannabaceae,Convolvulaceae, Chenopodiaceae, Crypthecodiniaceae, Cucurbitaceae,Ditrichaceae, Elaeagnaceae, Ericaceae, Euphorbiaceae, Fabaceae,Geraniaceae, Gramineae, Juglandaceae, Lauraceae, Leguminosae, Linaceae,Prasinophyceae or vegetable plants or ornamentals such as Tagetes.Examples which may be mentioned are the following plants selected fromthe group consisting of: Adelotheciaceae such as the generaPhyscomitrella, Anacardiaceae such as the genera Pistacia, Mangifera,Anacardium, Asteraceae, such as the genera Calendula, Carthamus,Centaurea, Cichorium, Cynara, Helianthus, Lactuca, Locusta, Tagetes,Valeriana, Apiaceae, such as the genus Daucus, Betulaceae, such as thegenus Corylus, Boraginaceae, such as the genus Borago, Brassicaceae,such as the genera Brassica, Melanosinapis, Sinapis, Arabadopsis,Bromeliaceae, such as the genera Ananas, Bromelia, Caricaceae, such asthe genus Carica, Cannabaceae, such as the genus Cannabis,Convolvulaceae, such as the genera Ipomea, Convolvulus, Chenopodiaceae,such as the genus Beta, Crypthecodiniaceae, such as the genusCrypthecodinium, Cucurbitaceae, such as the genus Cucurbita,Cymbellaceae such as the genera Amphora, Cymbella, Okedenia,Phaeodactylum, Reimeria, Ditrichaceae such as the genera Ditrichaceae,Astomiopsis, Ceratodon, Chrysoblastella, Ditrichum, Distichium,Eccremidium, Lophidion, Philibertiella, Pleuridium, Saelania, Trichodon,Skottsbergia, Elaeagnaceae such as the genus Elaeagnus, Ericaceae suchas the genus Kalmia, Euphorbiaceae such as the genera Manihot, Janipha,Jatropha, Ricinus, Fabaceae such as the genera Pisum, Albizia,Cathormion, Feuillea, Inga, Pithecolobium, Acacia, Mimosa, Medicago,Glycine, Dolichos, Phaseolus, Soja, Funariaceae such as the generaAphanorrhegma, Entosthodon, Funaria, Physcomitrella, Physcomitrium,Geraniaceae, such as the genera Pelargonium, Cocos, Oleum, Gramineae,such as the genus Saccharum, Juglandaceae, such as the genera Juglans,Wallia, Lauraceae, such as the genera Persea, Laurus, Leguminosae, suchas the genus Arachis, Linaceae, such as the genera Linum, Adenolinum,Lythrarieae, such as the genus Punica, Malvaceae, such as the genusGossypium, Marchantiaceae, such as the genus Marchantia, Musaceae, suchas the genus Musa, Onagraceae, such as the genera Camissonia, Oenothera,Palmae, such as the genus Elacis, Papaveraceae, such as the genusPapaver, Pedaliaceae, such as the genus Sesamum, Piperaceae, such as thegenera Piper, Artanthe, Peperomia, Steffensia, Poaceae, such as thegenera Hordeum, Secale, Avena, Sorghum, Andropogon, Holcus, Panicum,Oryza, Zea (maize), Triticum, Porphyridiaceae, such as the generaChroothece, Flintiella, Petrovanella, Porphyridium, Rhodella,Rhodosorus, Vanhoeffenia, Proteaceae, such as the genus Macadamia,Prasinophyceae such as the genera Nephroselmis, Prasinococcus,Scherffelia, Tetraselmis, Mantoniella, Ostreococcus, Rubiaceae such asthe genus Cofea, Scrophulariaceae such as the genus Verbascum,Solanaceae such as the genera Capsicum, Nicotiana, Solanum,Lycopersicon, Sterculiaceae, such as the genus Theobroma, or Theaceae,such as the genus Camellia.

More preferably, the plant is selected from the group of plant familiesAsteraceae, Brassicaceae, Chenopodiaceae, Euphorbiaceae, Gramineae,Leguminosae, and Malvaceae.

Especially preferred are for example the genera and species Brassicanapus, Brassica rapa ssp., Sinapis arvensis, Brassica juncea, Brassicajuncea var. juncea, Brassica juncea var. crispifolia, Brassica junceavar. foliosa, Brassica nigra, Brassica sinapioides, Melanosinapiscommunis, Brassica oleracea, Arabidopsis thaliana, Beta vulgaris, Betavulgaris var. altissima, Beta vulgaris var. Vulgaris, Beta maritima,Beta vulgaris var. perennis, Beta vulgaris var. conditiva or Betavulgaris var. esculenta, Phaeodactylum tricornutum, Pisum sativum, Pisumarvense, Pisum humile, Albizia berteriana, Albizia julibrissin, Albizialebbeck, Acacia berteriana, Acacia littoralis, Albizia berteriana,Albizzia berteriana, Cathormion berteriana, Feuillea berteriana, Ingafragrans, Pithecellobium berterianum, Pithecellobium fragrans,Pithecolobium berterianum, Pseudalbizzia berteriana, Acacia julibrissin,Acacia nemu, Albizia nemu, Feuilleea julibrissin, Mimosa julibrissin,Mimosa speciosa, Sericanrda julibrissin, Acacia lebbeck, Acaciamacrophylla, Albizia lebbek, Feuilleea lebbeck, Mimosa lebbeck, Mimosaspeciosa, Medicago sativa, Medicago falcata, Medicago varia, Glycine maxDolichos soja, Glycine gracilis, Glycine hispida, Phaseolus max, Sojahispida or Soja max, Hordeum vulgare, Hordeum jubatum, Hordeum murinum,Hordeum secalinum, Hordeum distichon, Hordeum aegiceras, Hordeumhexastichon, Hordeum hexastichum, Hordeum irregulare, Hordeum sativum,Hordeum secalinum, Secale cereale, Avena sativa, Avena fatua, Avenabyzantina, Avena fatua var. sativa, Avena hybrida, Sorghum bicolor,Sorghum halepense, Sorghum saccharatum, Sorghum vulgare, Andropogondrummondii, Holcus bicolor, Holcus sorghum, Sorghum aethiopicum, Sorghumarundinaceum, Sorghum caffrorum, Sorghum cernuum, Sorghum dochna,Sorghum drummondii, Sorghum durra, Sorghum guineense, Sorghumlanceolatum, Sorghum nervosum, Sorghum saccharatum, Sorghumsubglabrescens, Sorghum verticilliflorum, Sorghum vulgare, Holcushalepensis, Sorghum miliaceum, Panicum militaceum, Oryza sativa, Oryzalatifolia, Zea mays, Triticum aestivum, Triticum durum, Triticumturgidum, Triticum hybernum, Triticum macha, Triticum sativum orTriticum vulgare, Capsicum annuum, Capsicum annuum var. glabriusculum,Capsicum frutescens, Capsicum annuum, Nicotiana tabacum, Nicotianaalata, Nicotiana attenuata, Nicotiana glauca, Nicotiana langsdorffii,Nicotiana obtusifolia, Nicotiana quadrivalvis, Nicotiana repanda,Nicotiana rustica, Nicotiana sylvestris, Solanum tuberosum, Solanummelongena, Lycopersicon esculentum, Lycopersicon lycopersicum,Lycopersicon pyriforme, Solanum integrifolium or Solanum lycopersicum.

The most preferred plant species are Brassica napus, Brassica rapa,Brassica oleracea, Beta vulgaris, Medicago sativa, Glycine max Dolichossoja, Hordeum vulgare, Secale cereale, Avena sativa, Sorghum bicolor,Sorghum halepense, Sorghum saccharatum, Sorghum vulgare, Panicummilitaceum, Oryza sativa, Zea mays, Triticum aestivum, Triticum durum,Solanum tuberosum, Lycopersicon esculentum, and Gossypium hirsutum.

Transgenic plants may be obtained by transformation techniques aselsewhere in this specification. Preferably, transgenic plants can beobtained by T DNA-mediated transformation. Such vector systems are, as arule, characterized in that they contain at least the vir genes, whichare required for the Agrobacterium-mediated transformation, and thesequences which delimit the T-DNA (T-DNA border). Suitable vectors aredescribed elsewhere in the specification in detail.

Preferred mosses to be used as non-human transgenic organisms accordingto the present invention are Physcomitrella or Ceratodon. Preferredalgae to be used as non-human transgenic organisms according to thepresent invention are Isochrysis, Mantoniella, Ostreococcus orCrypthecodinium, and algae/diatoms such as Phaeodactylum orThraustochytrium.

The present invention relates to a polypeptide encoded by thepolynucleotide of the present invention.

The term “polypeptide” as used herein encompasses isolated oressentially purified polypeptides being essentially free of othercomponents. However, the term also encompasses polypeptide preparationscomprising the polypeptide of the present invention and other proteinsin addition. A polypeptide as used herein may by a chemically modifiedpolypeptide. Said modifications may be artificial modifications ornaturally occurring modifications. The polypeptide of the presentinvention shall have the activities referred to above. It can bemanufactured by chemical synthesis or recombinant molecular biologytechniques well known for the skilled artisan. Preferably, such a methodof manufacturing the polypeptide of the invention comprises (a)culturing the host cell of the present invention described elsewhereherein in more detail and (b) obtaining from the said host cell thepolypeptide of the present invention. In an aspect of this method, thepolypeptide can be obtained by conventional purification techniques froma lysate of the host cell including affinity chromatography, ionexchange chromatography, size exclusion chromatography, hydrophobicinteraction chromatography and/or preparative gel electrophoresis.Details on the manufacture and testing for the desired activities arealso found in the accompanying Examples below.

As indicated elsewhere herein, the polypeptide of the present inventioncan be applied in various genetic engineering procedures. Thus,contemplated in accordance with the present invention is, inter alia,the use of the polypeptide of the invention in a non-human organism and,preferably, a microorganism or plant, for integrating a heterologousnucleic acid of interest into a target nucleic acid molecule,preferably, into a genomic target DNA, such as a chromosome. Alsocontemplated is the use of the polypeptide of the invention in anon-human organism and, preferably, a microorganism or plant, forfacilitating the integration of a heterologous nucleic acid of interestinto a target nucleic acid molecule, preferably, into a genomic targetDNA, such as a chromosome. Preferably, the integration of the nucleicacid of interest will occur at the site of the tripartite DNArecognition site in the target nucleic acid molecule. Accordingly, thepolypeptide of the present invention can be, preferably, used fortargeted transgenesis (gene insertion), gene knock-out approaches (geneinactivation) or homologous replacement or knock-in approaches (genereplacement). In particular, the polypeptide of the present inventioncan also be used for the removal or inactivation of nucleic acids ofinterest from a genome, such as for the removal of marker genes used forthe selection of transgenic non-human organisms after the said selectionhas been carried out. Furthermore, the polypeptide of the presentinvention by allowing targeted transgenesis at a predetermined locusallows for controlling the integration site and the copy number of thetransgenes to be integrated.

Encompassed by the present invention is a method for introducing anucleic acid of interest into a genome of a non-human organismcomprising:

a) introducing into a non-human organism a nucleic acid of interest tobe introduced into the genome of the said organismb) expressing the polypeptide of the present invention in said organism;andc) cultivating said organism under conditions allowing said polypeptideto cleave the genome and allowing the nucleic acid of interest to becomeintroduced into the genome.

In the method of the present invention, a nucleic acid of interest,which shall be incorporated into the genome of a non-human organism asspecified elsewhere herein, is introduced into the said organism. Theintroduction of the nucleic acid of interest can be achieved by varioustransfection or transformation techniques as referred to elsewhereherein in more detail. A nucleic acid of interest as referred to hereinencompasses nucleic acids which shall be expressed by the non-humanorganisms, such as nucleic acids encoding proteins or RNAs, theproduction of which is envisaged, or nucleic acids which shall be usedto disrupt genes in the genome or shall be incorporated for any otherreason into the organisms genome.

The non-human organism according to the method of the present inventionshall express the polypeptide of the present invention. This can beachieved, preferably, by generating a transgenic non-human organismwhich comprises as a transgene either stably or transiently integratedthe polynucleotide of the present invention in an expressible form. Tothis end, the polynucleotide may be, preferably, transformed ortransfected into the organism comprised in an expression vector and,preferably, an expression vector of the invention as specified above.Moreover, the transgenic non-human organism to be applied in the methodof the present invention is selected from the group consisting of: amicroorganism, a plant, plant part or isolated cell thereof, or ananimal tissue or isolated cell thereof and, most preferably, is one ofthe non-human transgenic organisms of the invention as specifiedexplicitly elsewhere herein.

It will be understood that in the non-human transgenic organism to beused in the method of the invention, the polypeptide of the invention ispresent in a biologically active form, i.e. is capable of binding to thetripartite DNA recognition site and is capable of cleaving the DNA uponbinding within its DNA cleavage site. DNA binding and cleavage by thepolynucleotide of the invention can be achieved by culturing thenon-human transgenic organism for a time and under conditions whichallow for the said DNA binding and cleavage. Moreover, the non-humanorganism shall be cultured under conditions allowing for the integrationof the nucleic acid of interest into the cleaved genomic DNA. Suitableconditions can be applied by the skilled person without further ado and,in most cases, the integration of the nucleic acid of interest resultsfrom or is facilitated by endogenous DNA repair processes which aretriggered by the DNA cleavage elicited by the polypeptide of the presentinvention in the genome of the non-human organism. Preferred conditionswhich allow for DNA binding and cleavage are described in theaccompanying Examples below in more detail or can be derived from anyone of WO2003/080809, WO2000/46386, WO2009/006297, WO2006/074956,WO2006/134496, WO2007/148964, and/or WO2009/130695.

The present invention, finally, relates to a nucleic acid moleculecomprising the tripartite DNA recognition site of the polypeptide of thepresent invention.

Preferably, the said nucleic acid molecule is a nucleic acid of interestfor integration into a genome comprised, e.g., by a vector.Alternatively, the said nucleic acid molecule can be comprised in agenome into which the nucleic acid of interest as referred to aboveshall be integrated. The tripartite DNA recognition site comprised inthe aforementioned nucleic acid molecule is, preferably, a DNArecognition site comprising the recognition site of the first DNAbinding domain linked to the recognition site of the second DNA bindingdomain linked to the recognition site of the first DNA binding domain.

In a preferred embodiment, the nucleic acid molecule comprising thetripartite DNA recognition site of the polypeptide of the presentinvention comprises in 5′ to 3′ direction:

-   -   i. a DNA recognition site of a homing endonuclease,    -   ii. a first nucleic acid linker,    -   iii. a DNA recognition site of a restriction endonuclease,    -   iv. a second nucleic acid linker, and    -   v. the reverse complement sequence of a DNA recognition site of        a homing endonuclease.

Preferred homing endonucleases as well as preferred restrictionendonucleases are described elsewhere herein. Preferably, the homingendonuclease in (i) and (v) is a LAGLIDADG-family homing endonuclease ora variant thereof. More preferably, it is a I-SceI homing endonucleaseor of a variant thereof. Preferably, the restriction endonuclease in (v)is a type IIP restriction endonucleases. Most preferably, it is PvuII.

Thus, in a further preferred embodiment, the nucleic acid moleculecomprising the tripartite DNA recognition site comprises in 5′ to 3′direction:

-   -   i. a DNA recognition site of I-SceI,    -   ii. a first nucleic acid linker,    -   iii. a DNA recognition site of PvuII,    -   iv. a second nucleic acid linker, and    -   vi. the reverse complement sequence of a DNA recognition site of        I-SceI.

A preferred DNA recognition site of I-SceI is represented by bases 1 to18 of SEQ ID NO: 11. A preferred reverse complement sequence of a DNArecognition site of I-SceI is represented by bases 37 to 54 of SEQ IDNO: 11. The DNA recognition site of PvuII is represented by bases 25 to30 of SEQ ID NO: 11 (cagctg).

It is known homing endonucleases, including I-SceI, can tolerate smalldeviations (degenerations) of the nucleotide sequence of theirrecognition sites which nevertheless make recognition and cleavage bythe particular homing endonuclease possible. Thus, tripartite DNArecognition sites comprising 1, 2, 3 or 4 nucleotide exchanges in one orboth homing endonuclease recognition sites are also included here.

The said recognition sites shall be linked via a nucleic acid linkersequences comprising a number of nucleotides sufficient in length as toallow the specific binding of the homodimer of the polypeptide of thepresent invention (as set forth in ii. and iv.). The length of thenucleic acid linkers will depend on the size of the polypeptide of thepresent invention and, in particular, the length of the linker in thepolypeptide of the invention. Preferably, the nucleic acid linkerencompass between 1 to 20 in length, more preferably 4 to 8 nucleotidesin length, even more preferably between 5 and 7 nucleotides in length,and most preferably 6 nucleotides in length. The nucleotides of thelinker nucleic acids can be either identical or differ from each other.Preferably, the linker nucleic acid does, however, not interfere orinfluence DNA binding of the homodimer. Whether a nucleic acid linkerinfluences or interferes with the DNA binding can be determined by wellknown techniques.

In one embodiment, the tripartite DNA recognition site comprises anucleic acid sequence of:

a) a nucleic acid sequence as described by SEQ ID NO: 11, 12, or 13,b) a nucleic acid sequence differing by 1, 2, 3 or 4 bases from anucleic acid sequence as described by SEQ ID NO: 11, 12, or 13, thosedifferences being located at bases 1 to 18 of a sequence as described bySEQ ID NO: 11, 12, or 13,c) a nucleic acid sequence differing by 1, 2, 3 or 4 bases from anucleic acid sequence as described by SEQ ID NO: 11, 12, or 13, thosedifferences being located at bases 37 to 54 of a sequence as describedby SEQ ID NO: 11, 12, or 13,d) a nucleic acid sequence differing by 2, 3, 4, 5, 6, 7, or 8 basesfrom a nucleic acid sequence as described by SEQ ID NO: 11, 12, or 13,those differences being located at bases 1 to 18 and at bases 37 to 54of a sequence as described by SEQ ID NO: 11, 12, or 13, but not havingmore than 4 differing bases located at bases 1 to 18 and not more than 4differing bases located at bases 37 to 54.

Preferably, the tripartite DNA recognition site comprises a nucleic acidsequence as shown in SEQ ID NO: 11, 12, or 13.

Advantageously, the present invention provides for an artificialtripartite DNA recognition site which shall be not endogenously presentin a genome. Accordingly, integration of heterologous DNA can begoverned more precisely in non-human organisms carrying said tripartiteDNA recognition site as a result of DNA recombination techniques, e.g.,homologous recombination, at a certain desired locus.

Thus, contemplated in accordance with the present invention is, interalia, the use of the nucleic acid molecule comprising the tripartite DNArecognition site of the polypeptide of the present invention in anon-human organism and, preferably, a microorganism or plant, forintegration into a target nucleic acid molecule, preferably, into agenomic target DNA, such as a chromosome. Accordingly, the presentinvention also relates to a non-human organism comprising a nucleic acidmolecule comprising the tripartite DNA recognition site. Preferably, thenucleic acid molecule will also govern the integration of a nucleic acidmolecule in the target nucleic acid molecule. Accordingly, the saidnucleic acid molecule of the present invention can be, preferably, usedfor targeted transgenesis (gene insertion), gene knock-out approaches(gene inactivation) or homologous replacement or knock-in approaches(gene replacement). In particular, the nucleic acid molecule can also beused for the removal or inactivation of nucleic acids of interest from agenome, such as for the removal of marker genes used for the selectionof transgenic non-human organisms after the said selection has beencarried out. Furthermore, the nucleic acid molecule allows for targetedtransgenesis at a predetermined locus comprising it and, thus forcontrolling the integration site and the copy number of the transgenesto be integrated.

It will be understood that the present invention, consequently, alsocontemplates a vector comprising the aforementioned nucleic acidmolecule as well as a non-human organism comprising the said nucleicacid molecule.

Furthermore, preferably, the said nucleic acid molecule is applied inthe method of the invention and further comprises in addition to thetripartite DNA recognition site the nucleic acid of interest to beintegrate into the genome.

The definitions and explanations made for the vector, non-human organismand method above apply mutatis mutandis.

The present invention further relates to a non-human organism comprisingthe nucleic acid molecule comprising the tripartite DNA recognition siteas described above and polynucleotide encoding the polypeptide of thepresent invention. Preferably said organism is a microorganism, a plant,or an animal. Preferably, the plant is transformed with said nucleicacid molecule and/or said polynucleotide encoding the polypeptide of thepresent invention.

All references cited throughout this specification are herewithincorporated by reference with respect to their specific disclosurecontents discussed above and with respect to their entire disclosurecontents.

FIGURES

FIG. 1 shows an agarose gel analysis for determining cleavage productsof the L(6) (SEQ ID NO: 9) variants of the polypeptide of the presentinvention at different time points after beginning of the incubation.The kinetic analysis revealed no cleavage at unspecific sites even after21 hours of digestion.

FIG. 2 shows an agarose gel analysis for determining cleavage productsof the L(6) (SEQ ID NO: 9) and L(+) (SEQ ID NO: 10). variants of thepolypeptide of the present invention at various differentconcentrations. The enzyme titration revealed unspecific cleavage onlyat a concentration of 8-32× molar excess of enzyme over DNA for the L(6)variant.

FIG. 3 shows an agarose gel analysis for determining cleavage productsof the L(6) (SEQ ID NO: 9) and L(+) (SEQ ID NO: 10) variants of thepolypeptide of the present invention in the presence or absence ofbacteriophage lambda competitor DNA. Cleavage occurs independently ofthe presence of bacteriophage lambda DNA.

FIG. 4 shows an electrophoretic mobility shift analysis (EMSA). (A) thetripartite DNA recognition site I-SceI-PvuII-I-SceI is bound by thefusion protein L(6); (b) and (C) no binding occurs at only the I-SceIDNA recognition site (B) or the PvuII DNA recognition site (C).

FIG. 5 shows an in vivo analysis for fusion protein activity. E. colicells were transformed with a plasmid coding for the companionmethyltransferase of PvuII. Either a plasmid encoding wild type PvuII,the L(6) fusion protein or the L(+) fusion protein was cotransformed.The fusion protein showed surviving colonies in the absence ofmethyltransferase demonstrating that the fusion protein does not attackunmethylated (i.e. unprotected) PvuII sites.

FIG. 6 shows an agarose gel analysis for determining the activity ofshortened variants of the L(6) (SEQ ID NO: 9) and L(+) (SEQ ID NO: 10)fusion proteins. No difference was observed.

The following sequences referred to herein are shown in the accompanyingsequence listing:

SEQ ID NO: 1: amino acid sequence of I-SceI;SEQ ID NO: 2: amino acid sequence of PvuII;

SEQ ID NO: 3: Linker ASRTTG SEQ ID NO: 4: Linker ASTKQLVKSG SEQ ID NO:5: Linker ASGGSGSGSG SEQ ID NO: 6: Linker ASGDSGSDSG

SEQ ID NO: 7: nucleic acid sequence encoding fusion proteinP_((T46G, Y94F))-L₍₆₎-Ss*;SEQ ID NO: 8: nucleic acid sequence encoding fusion proteinP_((T46G, Y94F))-L₍₊₎-Ss*;SEQ ID No: 9: amino acid sequence of fusion proteinP_((T46G, Y94F))-L₍₆₎-Ss*;SEQ ID NO: 10: amino acid sequence of fusion proteinP_((T46G, Y94F))-L₍₊₎-Ss*;SEQ ID NO: 11: nucleic acid sequence for the tripartite DNA recognitionsite of the aforementioned fusion proteins:

TAGGGATAACAGGGTAATGGTACTCAGCTGATTCATATTACCCTGTTATCCCTA.

SEQ ID NO: 12: nucleic acid sequence for the tripartite DNA recognitionsite of the aforementioned fusion proteins:

TAGGGATAACAGGGTAATATGAATCAGCTGAGTACCATTACCCTGTTATCCCTA

SEQ ID NO: 13: nucleic acid sequence for the tripartite DNA recognitionsite of the aforementioned fusion proteins:

TAGGGATAACAGGGTAATNNNNNNCAGCTGNNNNNNATTACCCTGTTATCCCTA,

wherein n can be A, T, C or G

EXAMPLES

The following Examples illustrate the invention and shall not,whatsoever, be construed as limiting the scope.

Example 1 Cloning of Different Fusion Proteins of I-SceI and PvuII

The PvuII-I-SceI fusion enzyme was created by fusing PvuII via itsC-terminus to the N-terminus of a catalytically inactive variant ofI-SceI (Gruen 2002, Nucleic Acids Res; 30(7):e29.) which was truncatedat the C-terminus (corresponding to the co-crystal structure, Moure2003, J. Mol. Biol. 334 (4) 685-95). For this the genes coding for PvuIIwas connected via its C-terminal His₆-tag to the gene coding forI-SceI_((D44S))ΔC9 and cloned into the vector pASK-IBA63b-plus (IBA)coding for a C-terminal Strep-tag. For further improvement the twoactive site residues (D44 and D145) of I-SceI were mutated according toLippow 2009, Nucleic Acid Res 37(9): 3061-3073 via PCR-based directedmutagenesis (Kirsch 1998, Nucleic Acids Res. 26 (7) 1848-50). Theresulting variants were later on called S* (I-SceI_D44N, D145A) and Ss*(I-SceIΔC9_D44N, D145A). The mutagenesis of certain residues of PvuIIwas performed in the same way for the fusion enzymes. To have a buildingblock like architecture for the linker region between the genes forPvuII and I-SceI three restriction enzyme sites (NheI, BsiWI, AgeI) wereintroduced between these two gene instead of the His6-tag (L_((H)))leading to L₍₆₎ (SEQ ID No: 3). By cleaving the resulting vector withNheI and AgeI the linker L_((N)) (SEQ ID NO: 5), L₍₊₎ (SEQ ID NO: 4) andL⁽⁻⁾ (SEQ ID NO: 6) having complementary ends could be cloned into thesesites.

Example 2 Functional Characterization of Different Fusion Proteins

8 nM linearized plasmid DNA containing the tripartite site (S6P6S) andan additional unaddressed PvuII-site were incubated with 8 nM of theL(6) variant of the fusion enzyme (SEQ ID NO: 9) in optimized KG Buffer(100 mM potassium glutamate, 25 mM Tris-acetate, 0.8 mM Mg-acetate, 100mM KCl, 500 μM 2-mercaptoethanol, 10 μg/ml BSA). This buffer is used forall further experiments as well. After certain time points a sample ofthe cleavage reaction was withdrawn, the reaction stopped by addingloading buffer and analyzed on agarose gel. The results are shown inFIG. 1.

8 nM linearized plasmid DNA containing the addressed site with anadditional unaddressed PvuII site (S6P6S_P; A) or supercoiled plasmidDNA containing just a PvuII site (B) were incubated with fusion enzymeranging from 4-256 nM in optimized KG Buffer overnight (˜16 h). Thereactions were analyzed on 0.8% agarose gels. Results are shown in FIG.2.

8 nM linearized plasmid DNA (S6P6S_P) were incubated with 8 nM fusionenzyme in optimized KG Buffer for 3 h at 37° C. either in the presenceor absence of 940 pM λ-DNA which contains 15 PvuII sites. The reactionwas analyzed on 0.8% agarose gel. Results are shown in FIG. 3.

For the determination of binding constants of the fusion enzymes, EMSAswith radioactive labeled PCR-fragments were done. The shift fragmentswere created via PCR using [α³²P] dATP. One fragment contained theaddressed site (S6P6S; A), just an I-SceI site (S; B) or just a PvuIIsite (P; C). 2 nM of the radiolabeled substrate were incubated withfusion enzyme at concentrations ranging from 1-150 nM in optimized KGBuffer without magnesium for 30 min at room temperature. After adding 1μl 87% glycerol the samples were loaded onto a 6% polyacrylamidTris-Acetate (pH 8.5) gel and run for 2 h at 10V/cm. The bands werevisualized using the InstantImager system (Packard). Results are shownin FIG. 4.

Electrocompetent E. coli cells either harboring the plasmid coding forM.PvuII or not were transformed with 50 ng plasmid coding for PvuII_wtor one of the fusion enzymes. 50 μl of the transformation mixture werespread on agar-plates containing the corresponding antibiotics andincubated overnight at 37° C. Results are shown in FIG. 5.

8 nM linearized plasmid DNA (S6P6S_P) were incubated with 8 nM of thefusion enzymes with the ΔC9 I-SceI (SEQ ID 9 &10) or the fusion enzymeswith full length I-SceI in optimized KG Buffer for 1 h at 37° C. Thereactions were analyzed on 0.8% agarose gels. Results are shown in FIG.6.

1-18. (canceled)
 19. A polynucleotide encoding a polypeptide comprising:(i) a first module comprising at least a first DNA binding domainderived from a homing endonuclease; (ii) a linker; and (iii) a secondmodule comprising at least a second DNA binding domain and a cleavagedomain derived from a restriction endonuclease; wherein said polypeptidefunctionally interacts only with DNA comprising a DNA recognition sitefor the first DNA binding domain and a DNA recognition site for thesecond DNA binding domain, and wherein said cleavage domain cleaves DNAwithin a specific DNA cleavage site upon binding of the polypeptide. 20.The polynucleotide of claim 19, wherein said specific DNA cleavage siteand said DNA recognition site of the second DNA binding domain of therestriction endonuclease are identical.
 21. The polynucleotide of claim19, wherein said second DNA binding domain and the cleavage domaincomprised in the second module are derived from a type IIP restrictionendonuclease.
 22. The polynucleotide of claim 19, wherein said secondDNA binding domain and the cleavage domain comprised in the secondmodule are derived from a restriction endonuclease which exhibitsreduced DNA binding and/or reduced catalytic activity when compared tothe wild type restriction endonuclease.
 23. The polynucleotide of claim19, wherein said second DNA binding domain and the cleavage domaincomprised in the second module are derived from PvuII.
 24. Thepolynucleotide of claim 23, wherein said second DNA binding domain andthe cleavage domain comprised in the second module comprise at least oneof following modifications: substitution T46G, substitution H83A,substitution Y94F, substitution T46G in combination with H83A,substitution T46G in combination with Y94F or substitution T46G incombination with H83A and Y94F.
 25. The polynucleotide of claim 19,wherein said first module exhibits reduced or no catalytic activity. 26.The polynucleotide of claim 19, wherein said first DNA binding domaincomprised in the first module is derived from a LAGLIDADG-family homingendonuclease.
 27. The polynucleotide of claim 26, wherein said first DNAbinding domain comprised in the first module is derived from I-SceI. 28.The polynucleotide of claim 27, wherein said first DNA binding domaincomprised in the first module comprise at least one of followingmodifications: substitution D44S alone or in combination with D145A, orsubstitution D44N in combination with D145A.
 29. The polynucleotide ofclaim 19, wherein said linker consists essentially of 6 to 10 aminoacids.
 30. The polynucleotide of claim 29, wherein said linker has anamino acid sequence of SEQ ID NO: 3 or SEQ ID NO:
 4. 31. A vectorcomprising the polynucleotide of claim
 19. 32. A non-human organismcomprising the polynucleotide of claim
 19. 33. A polypeptide encoded bythe polynucleotide of claim
 19. 34. A nucleic acid molecule comprisingin 5′ to 3′ direction: i. a DNA recognition site of I-SceI, ii. a firstnucleic acid linker, iii. a DNA recognition site of PvuII, iv. a secondnucleic acid linker, and v. the reverse complement sequence of a DNArecognition site of I-SceI.
 35. A vector comprising the polynucleotideof claim
 34. 36. A non-human transgenic organism comprising thepolynucleotide of claim
 34. 37. A non-human transgenic organismcomprising the polynucleotide of claim 19 and further comprising anucleic acid molecule comprising in 5′ to 3′ direction: i. a DNArecognition site of I-SceI, ii. a first nucleic acid linker, iii. a DNArecognition site of PvuII, iv. a second nucleic acid linker, and v. thereverse complement sequence of a DNA recognition site of I-SceI.
 38. Amethod for introducing a nucleic acid of interest into a genome of anon-human organism comprising: a) introducing into a non-human organisma nucleic acid of interest to be introduced into the genome of the saidorganism b) expressing the polypeptide of claim 33 in said organism; andc) cultivating said organism under conditions allowing said polypeptideto cleave the genome and allowing the nucleic acid of interest to becomeintroduced into the genome.
 39. The method of claim 38, wherein saidnon-human transgenic organism is selected from the group consisting of:a microorganism, a plant, plant part or isolated cell thereof, or ananimal tissue or isolated cell thereof.
 40. The non-human transgenicorganism of claim 38, wherein said non-human transgenic organism isselected from the group consisting of: a microorganism, a plant, plantpart or isolated cell thereof, or an animal tissue or isolated cellthereof.
 41. The non-human transgenic organism of claim 36, wherein saidnon-human transgenic organism is selected from the group consisting of:a microorganism, a plant, plant part or isolated cell thereof, or ananimal tissue or isolated cell thereof.